US5402894A - Coal conditioning process - Google Patents

Coal conditioning process Download PDF

Info

Publication number
US5402894A
US5402894A US08/138,409 US13840993A US5402894A US 5402894 A US5402894 A US 5402894A US 13840993 A US13840993 A US 13840993A US 5402894 A US5402894 A US 5402894A
Authority
US
United States
Prior art keywords
coal
dewatering
filter cake
slurry
wash water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US08/138,409
Inventor
Mary A. Winterhoff
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chemical Dewatering Technology Inc
Original Assignee
Chemical Dewatering Technology Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chemical Dewatering Technology Inc filed Critical Chemical Dewatering Technology Inc
Priority to US08/138,409 priority Critical patent/US5402894A/en
Assigned to CHEMICAL DEWATERING TECHNOLOGY, INC. reassignment CHEMICAL DEWATERING TECHNOLOGY, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WINTERHOFF, MARY ANNE
Application granted granted Critical
Publication of US5402894A publication Critical patent/US5402894A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/08Subsequent treatment of concentrated product
    • B03D1/10Removing adhering liquid from separated materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03BSEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
    • B03B9/00General arrangement of separating plant, e.g. flow sheets
    • B03B9/005General arrangement of separating plant, e.g. flow sheets specially adapted for coal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/008Organic compounds containing oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/02Froth-flotation processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/007Modifying reagents for adjusting pH or conductivity
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2203/00Specified materials treated by the flotation agents; specified applications
    • B03D2203/02Ores
    • B03D2203/04Non-sulfide ores
    • B03D2203/08Coal ores, fly ash or soot

Landscapes

  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Abstract

A process for improving the efficiency of coal dewatering and deashing uses complexing agents such as sodium gluconate in alkaline solution to form soluble compounds with cations such as Al+3, Fe+3, Mg+2, and Ca+2. The formation of such compounds reduces the adsorption and/or desorbs clay slimes from the coal surface.

Description

BACKGROUND OF THE INVENTION
I. Field of the Invention
Many commercially important coal measures contain substantial proportions of ash. Almost all uses of coal can be accomplished more efficiently by reducing the moisture and ash content of the coal. Especially where the coal is used for generation of heat or electrical power, the moisture content should be reduced to the lowest practical level, and the higher heating value should be as high as possible. Reductions in moisture and ash content produce corresponding increases in the higher heating value of the coal.
My invention relates to a novel chemical coal conditioning process which uses complexing agents such as sodium gluconate in alkaline solution to form soluble compounds with cations such as Al+3, Fe+3, Mg+2, and Ca+2. I have found that the formation of such compounds reduces the adsorption and/or desorbs clay slimes from the coal surface. In a preferred embodiment of my invention, deashing and dewatering is further enhanced by addition of surfactants such as those disclosed in my co-pending application, Ser. No. 8-047787 filed Apr. 15, 1993, the disclosure of which is incorporated herein by reference.
II. Description of the Prior Art
Some information is available concerning the chemistry of clay/coal interaction. In Burdon, R. G.; Booth, R. W. and Mishra, S. K., "Factors Influencing the Selection of Process for the Benificiation of Fine Coal", Proceedings of the 7th International Coal Preparation Congress, Sydney, N.S.W., Australia, Paper E.1 (1976), for example, a theoretical discussion of the mechanisms of clay adsorption on the organic constituents of coal is presented, and it is hypothesized that Fe+3 and Al+3 cations play a role in promoting such adsorption. Eamer, B. J., "Surface Chemical Treatment of Fine Coal With Slime Problem", M. P. Appl. Sc. Thesis, Western Australian Institute of Technology (1981) and Mishra, S. K. and Eamer, B. T., "Effect of Clay Slimes On Flotation Behavior of Coal", Paper presented at the Fine Particle Society Conference (1985) include similar discussions.
Conventional dewatering and deashing processes may use a rotary drum vacuum filter or comparable device to remove ash and water from slurries of fine coal. A variety of chemical pretreatments have been disclosed to improve the performance of these process steps. U.S. Pat. No. 5,192,338 (Waugh), for example, discloses a treating process using serial treatment with aqueous solutions of citric acid and glycerol at elevated temperature for a period of 30 to 45 minutes to beneficiate coal. Mention is made of the use of "organic complexing agents capable of complexing with metal cations" (col. 3, lines 38-39 and 51-56), but the only reagents disclosed in that category are ethylene diamine tetraacetic acid and its disodium salt; 8-hydroxyquinoline and mercaptoethanol.
U.S. Pat. No. 5,089,142 discloses using sodium hexametaphosphate to control slime formation in centrifugal dewatering processes.
Some investigators, as in U.S. Pat. No. 4,231,868 (Wang, et. al.), have suggested adding sulfosuccinate surfactants to slurries of fine coal in order to improve dewatering efficiency. A similar approach was suggested in U.S. Pat. No. 4,985,162 (Cole). Other researchers also have suggested using sulfur and nitrogen-based compounds, as in U.S. Pat. No. 4,897,201 (Yamomoto, et. al.). The introduction of sulfur-containing surfactants into the coal/water slurry, however, requires application rates substantially higher than those used in my invention. Such surfactants also cause undesirable foam formation downstream of the filtration operation that interferes with subsequent coal processing. Therefore, additional anti-foaming agents may be required. The addition of sulfur to the processed coal is also undesirable from an air pollution standpoint.
Still other investigators have suggested the addition of other reagents to the coal/water slurry. A quaternary amine surfactant was suggested in U.S. Pat. No. 4,892,663 (Keys). U.S. Pat. No. 4,290,897 discloses the addition of organopolysiloxanes and U.S. Pat. No. 4,447,344 (Roe) discloses a variety of ethoxylated alcohols.
None of these references, alone or in combination, suggests that the effectiveness of the coal cleaning processes can be improved by using any complexing agents in basic solution, or by following such treatment with the addition of surfactants such as sodium laureth-13 carboxylate salt in aqueous solution in the form of a foam.
SUMMARY OF THE INVENTION
Improving the effectiveness of specific gravity separation of clay slimes from coal appears to depend upon reducing or preventing the adsorption of the clay slimes onto the organic matrix of the coal itself, and/or desorbing the clay slimes from the coal surface. I have found that the extent to which clay slimes adsorb onto the coal particles can be reduced and/or desorbed by treatment with certain complexing agents; most preferably, with sodium gluconate at low concentration in basic solution. Such pretreatment can be followed advantageously with the addition of a foam made from aqueous solutions of surfactants, preferably sodium laureth 13 carboxylate, to the filter cake which is formed during a subsequent dewatering operation. The combination has been found to provide more effective deashing and dewatering than is obtainable by the use of either an organic complexing agent alone, or by means of a surfactant alone.
Accordingly, one object of my invention is to provide a coal dewatering and deashing process that uses sodium gluconate or related molecules in a basic solution substantially at room temperature to react with various cations, forming water-soluble complexes that prevent the adsorption and/or desorb clay slimes from the organic coal matrix, thereby improving the efficiency of the coal cleaning process.
Another object of my invention is to provide a coal dewatering and deashing process that avoids the use of sulfur-containing surfactants by applying a foamed chemical dewatering agent such as sodium laureth-13 carboxylate salt directly to the permeable cake following pretreatment with a complexing agent in a basic solution, to achieve significant ash and moisture content reductions.
DETAILED DESCRIPTION OF THE INVENTION
In the process of my invention, coal is washed in a conventional coal washing facility, which typically segregates the coal based on particle size. Fine coals are separated from coarse coals and continue through the washing process. Fine coal of -28 mesh typically is further washed using a froth flotation step followed by vacuum filtration of the overhead from the froth filtration operation.
My improvements comprise: (1) the addition to the wash water of a basic (alkaline) aqueous solution of a complexing agent capable of complexing with the cations that are naturally present; and (2) the application to the surface of a permeable cake of a dewatering foam made from aqueous solutions of carboxylic acid or carboxylate salts according to the process of my copending application Ser. No. 8-047787 filed Apr. 15, 1993, the disclosure of which is incorporated herein by reference. Complexing agent addition alone improves the results of conventional deashing and dewatering operations; still further improvement is obtained by complexing agent addition followed by the use of a dewatering foam.
More specifically, I have found that the following complexing agents can be used to improve the efficiency of dewatering, ash removal and increase the yield of clean coal: gluconic acid, glucaric acid, gulonic acid, glucoheptonic acid and glucuronic acid as well as their sodium and potassium salt forms. It should be understood that other additional reagents could be added to promote the deashing of the coal. Such other promoter reagents include: ethylene diamine tetraacetic acid (EDTA), pyrophosphate, hexameta phosphate, hydroxy ethylidene diphosphonic acid, amino methylene tri phosphonic acid, phosphonobutane tricarboxylic acid, hexa methylene diamine tetra phosphonic acid, polyacrylic acids, polymethacrylate, acrylate-acrylamide copolymer and maleic anhydride copolymer.
The concentration of complexing agent following its addition to the wash water should be between about 50 and 5000 lbs of active complexing agent per one million lbs of wash water. The most preferred complexing agent concentration corresponds to a loading of approximately 500 lbs of active complexing agent per one million lbs of wash water. The amount of complexing agent required depends upon the specific complexing agent used the coal chemistry, the hardness of the wash water, and the solution pH. However, the specific application can be optimized by using simple laboratory testing procedures.
At the time the complexing agent is added, the pH of the wash water should be adjusted to between about 7.0 and 12.0, and most preferably about 9.0 by addition of suitable bases (e.g., NaOH or KOH).
The complexing reactions will be sufficiently complete within about 5 minutes from the time the coal contacts the wash water. Reaction times can be further shortened by altering concentration and/or pH.
In the preferred embodiment of my invention, the next processing step is continued washing and separation of coal particles based on particle size. Finer particles (minus 1/4 inch) are separated from coarse particles for further processing and/or dewatering. Typically, coal particles ranging in size from minus 1/4 inch to plus 28 mesh are next dewatered using modified screen bowl centrifuges. The minus 28 mesh coal is further washed using a froth flotation cell. The froth removed from the top of the froth flotation cell is then dewatered via rotary drum vacuum filtration. The effectiveness of dewatering using centrifugal dryers and rotary vacuum systems can be enhanced by using the dewatering foam technique described in my copending application Ser. No. 8-047787 filed Apr. 15, 1993. Any of the dewatering foams disclosed in that application can be used in the process of this invention following the complexing and froth flotation steps.
Laboratory tests were performed to determine quantitatively the performance of certain specific embodiments of my invention. The examples are solely illustrative and do not restrict the scope of my invention.
EXAMPLE 1
About 2750 ml. of aqueous solution containing approximately 1000 ppm of 50 wt % gluconic acid was prepared. Its pH was raised to about 9.0 by adding NaOH. Approximately 250 grams of -28 mesh bituminous Elkhorn no. 2 coal was added. The slurry was mixed and aerated for 5 minutes. The duration of the mixing was selected to duplicate the residence time associated with actual froth flotation cell used at coal processing facilities. After 5 minutes, about 2 ml. of kerosene was added to the slurry and the froth was removed using a collection header attached to a vacuum system. The collected froth was dewatered using a standard vacuum filtration system.
A blank was run under the foregoing conditions without gluconic acid. The results of these test were:
______________________________________                                    
           % ash dry basis                                                
______________________________________                                    
Blank        9.36                                                         
Treated      6.34                                                         
______________________________________                                    
Thus, the washed coal that was exposed to gluconic acid treatment had about 56% less ash.
EXAMPLE 2
Two blanks and a treated sample were prepared using the procedure of Example 1. Residue from the bottom was collected and analyzed for ash content. The results were:
______________________________________                                    
           % ash dry basis                                                
______________________________________                                    
Blank 1      24.86                                                        
Treated      35.54                                                        
Blank 2      25.71                                                        
______________________________________                                    
The increased ash content of the residue further demonstrates that more of the organic matrix of the coal was liberated from the ash, thereby decreasing the ash content and increasing the yield of the washed coal.
EXAMPLE 3
A blank and a treated sample were prepared as described in Example 1. The collected coal removed as froth was then dewatered using a Buchner funnel system controlled at a 15" Hg vacuum for 1 minute. Approximately 0.45 lbs of foamed dewatering agent (specifically, sodium laureth 13 carboxylate) per ton of dry coal was applied as a foam at a 10:1 expansion ratio to both the blank and the gluconic acid-treated sample using the process described in my copending application Ser. No. 8-047787. The results were:
______________________________________                                    
                    % moisture                                            
______________________________________                                    
Blank                 35.3                                                
Blank with dewatering foam                                                
                      30.1                                                
Treated sample        32.5                                                
Treated sample with dewatering foam                                       
                      18.6                                                
______________________________________                                    
Thus, the addition of pretreatment with gluconic acid complexing agent to the process of my copending application Serial No. 8-047787 produces a further 43% improvement in dewatering efficiency.
It will be apparent to those of ordinary skill in the art that changes and modifications could be made while remaining within the scope of my invention. For example, other foamed dewatering agents could be used, as disclosed in my copending application Ser. No. 9-047787 It is my intention, therefore, to cover all such equivalent processes, and to limit my invention only as specifically set forth in the following claims.

Claims (6)

I claim:
1. A process for conditioning coal that contains an undesirable clay mineral prior to dewatering and deashing, comprising:
(a) preparing a slurry of wash water and coal;
(b) adding to said slurry a basic aqueous solution of a complexing agent capable of reacting with said undesirable clay mineral to form a water soluble complex, wherein said basic solution has a pH of between about 7 and 12, wherein the concentration of said complexing agent in said wash water is between about 50 and 5000 lbs per one million lbs of wash water, and;
(c) allowing sufficient time at ambient temperature for formation of said water soluble complex;
(d) separating coal from said slurry by froth flotation;
(e) forming a filter cake from said separated coal;
(f) drying said filter cake;
(g) applying a dewatering foam to said filter cake during the process of cake drying; and
(h) completing the filtration of said filter cake.
2. A process for conditioning coal that contains an undesirable clay mineral prior to dewatering and deashing, comprising:
(a) preparing a slurry of wash water and coal;
(b) adding to said slurry a basic aqueous solution of a complexing agent capable of reacting with said undesirable clay mineral to form a water soluble complex, wherein said basic solution has a pH of between about 7 and 12, wherein the concentration of said complexing agent in said wash water is between about 50 to 5000 lbs per one million lbs of wash water, and;
(c) allowing sufficient time at ambient temperature for formation of said water soluble complex;
(d) separating coal from said slurry by froth flotation;
(e) forming a filter cake from said separated coal;
(f) drying said filter cake;
(g) applying a dewatering foam to said filter cake during the process of cake drying; and
(h) completing the filtration of said filter cake.
3. A process for conditioning coal that contains an undesirable clay mineral prior to dewatering and deashing, comprising:
(a) preparing a slurry of wash water and coal;
(b) adding to said slurry a basic aqueous solution of a complexing agent capable of reacting with said undesirable clay mineral to form a water soluble complex, wherein said basic solution has a pH of between about 7 and 12, wherein the concentration of said complexing agent in said wash water is between about 50 to 5000 lbs per one million lbs of wash water, and;
(c) allowing sufficient time at ambient temperature for formation of said water soluble complex;
(d) separating coal from said slurry by froth flotation;
(e) forming a filter cake from said separated coal;
(f) drying said filter cake;
(g) applying a dewatering foam to said filter cake during the process of cake drying; and
(h) completing the filtration of said filter cake.
4. A process for conditioning coal that contains an undesirable clay mineral prior to dewatering and deashing, comprising:
(a) preparing a slurry of wash water and coal;
(b) adding to said slurry a basic aqueous solution of a complexing agent capable of reacting with said undesirable clay mineral to form a water soluble complex;
(c) allowing sufficient time at ambient temperature for formation of said water soluble complex;
(d) separating coal from said slurry by froth flotation;
(e) forming a filter cake from said separated coal;
(f) drying said filter cake;
(g) applying a dewatering foam to said filter cake during the process of cake drying, where said dewatering foam is made from an aqueous solution of a dewatering agent and contains between about 0.1 wt % dewatering agent and about 1.0 wt % of said dewatering agent, wherein said dewatering agent is sodium laureth-13 carboxylate; and
(h) completing filtration of said filter cake.
5. A process for conditioning coal that contains an undesirable clay mineral prior to dewatering and deashing, comprising:
(a) preparing a slurry of wash water and coal;
(b) adding to said slurry a basic aqueous solution of a complexing agent capable to reacting with said undesirable clay mineral to form a water soluble complex, wherein the pH of said basic solution is between about 7 and 12, the concentration of said complexing agent in said wash water is between about 50 to 5000 lbs of active complexing agent per one million lbs of wash water; and wherein said complexing agent is gluconic acid;
(c) allowing sufficient time at ambient temperature for formation of said water soluble complex;
(d) separating coal from said slurry by froth flotation; and
(e) dewatering said coal through the use of a dewatering foam wherein the step of dewatering said coal through the use of a dewatering foam comprises
(f) forming a filter cake from said separated coal;
(g) drying said filter cake;
(h) applying a dewatering foam to said filter cake during the process of cake drying, where said dewatering foam is made from an aqueous solution of a dewatering agent and contains between about 0.1 wt % dewatering agent and about 1.0 wt % of said dewatering agent; and
(i) completing filtration of said filter cake.
6. A process for conditioning coal that contains an undesirable clay mineral prior to dewatering and deashing, comprising:
(a) preparing a slurry of wash water and coal;
(b) adding to said slurry a basic aqueous solution of a complexing agent capable of reacting with said undesirable clay mineral to form a water soluble complex, wherein the pH of said basic solution if between about 7 and 12, the concentration of said complexing agent in said wash water is between about 50 to 5000 lbs of active complexing agent per one million lbs of wash water; and wherein said complexing agent is gluconic acid;
(c) allowing sufficient time at ambient temperature for formation of said water soluble complex;
(d) separating coal from said slurry by froth flotation; and
(e) forming a filter cake from said separated coal;
(f) drying said filter cake;
(g) applying a dewatering foam to said filter cake during the process of cake drying, wherein said dewatering foam is made from an aqueous solution of a dewatering agent and contains between about 0.1 wt % dewatering agent and about 1.0 wt % of said dewatering agent; wherein said dewatering agent is sodium laureth-13 carboxylate and
(h) completing filtration of said filter cake.
US08/138,409 1993-10-18 1993-10-18 Coal conditioning process Expired - Fee Related US5402894A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US08/138,409 US5402894A (en) 1993-10-18 1993-10-18 Coal conditioning process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/138,409 US5402894A (en) 1993-10-18 1993-10-18 Coal conditioning process

Publications (1)

Publication Number Publication Date
US5402894A true US5402894A (en) 1995-04-04

Family

ID=22481871

Family Applications (1)

Application Number Title Priority Date Filing Date
US08/138,409 Expired - Fee Related US5402894A (en) 1993-10-18 1993-10-18 Coal conditioning process

Country Status (1)

Country Link
US (1) US5402894A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5799882A (en) * 1996-02-21 1998-09-01 Klimpel; Richard R. Hydroxy-carboxylic acid grinding aids
US6135372A (en) * 1996-02-21 2000-10-24 Klimpel; Richard R. Hydroxy-carboxylic acid grinding aids
WO2007021213A1 (en) * 2005-08-15 2007-02-22 Obschestvo S Ogranichennoy Otvetstvennostyu 'mezdunarodny Nauchny Tsentr Po Teplophizike I Energetike' Coal dressing method and device for carrying out said method
RU2500480C2 (en) * 2012-02-20 2013-12-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Иркутский государственный технический университет" (ФГБОУ ВПО "ИрГТУ") Method for extraction of nano-sized particles from man-made wastes by flotation
WO2015103316A1 (en) * 2013-12-31 2015-07-09 Omnis Mineral Technologies, Llc Vibration assisted vacuum dewatering of fine coal particles
CN112147299A (en) * 2020-09-22 2020-12-29 中国矿业大学(北京) Method and device for detecting content of clay minerals

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB159285A (en) * 1919-11-20 1921-02-21 Edwin Edser Improvements in or relating to the treatment of materials containing coal
GB272301A (en) * 1926-03-12 1927-06-13 Percy Thomas Williams Improvements in or relating to the froth-flotation concentration of coal
US1944529A (en) * 1931-09-26 1934-01-23 Erz Und Kohle Flotation Gmbh Flotation process
US4162966A (en) * 1976-06-16 1979-07-31 Nalco Chemical Company Flotation of deep mined coal with water-in-oil emulsions of sodium polyacrylate
US4211642A (en) * 1979-01-05 1980-07-08 Vojislav Petrovich Beneficiation of coal and metallic and non-metallic ores by froth flotation process using polyhydroxy alkyl xanthate depressants
EP0020275A1 (en) * 1979-06-01 1980-12-10 Calgon Corporation Process for improving the recovery of clean coal from flotation circuits
US4253944A (en) * 1979-12-28 1981-03-03 The Dow Chemical Company Conditioner for flotation of oxidized coal
US4278533A (en) * 1980-02-07 1981-07-14 The Dow Chemical Company Conditioner for flotation of oxidized coal
US4305815A (en) * 1979-12-28 1981-12-15 The Dow Chemical Company Conditioner for flotation of oxidized coal
US4474619A (en) * 1979-01-25 1984-10-02 The Dow Chemical Company Conditioner for flotation of coal
US4537599A (en) * 1983-04-28 1985-08-27 Greenwald Sr Edward H Process for removing sulfur and ash from coal
GB2163975A (en) * 1984-09-06 1986-03-12 American Cyanamid Co Froth flotation of coal
US4604099A (en) * 1984-01-30 1986-08-05 Ciba-Geigy Corporation Process for printing cellulose-containing textile material with foam-containing reactive dyes and addition of (meth) acrylamide polymers
US4732669A (en) * 1986-07-21 1988-03-22 The Dow Chemical Company Conditioner for flotation of coal

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB159285A (en) * 1919-11-20 1921-02-21 Edwin Edser Improvements in or relating to the treatment of materials containing coal
GB272301A (en) * 1926-03-12 1927-06-13 Percy Thomas Williams Improvements in or relating to the froth-flotation concentration of coal
US1944529A (en) * 1931-09-26 1934-01-23 Erz Und Kohle Flotation Gmbh Flotation process
US4162966A (en) * 1976-06-16 1979-07-31 Nalco Chemical Company Flotation of deep mined coal with water-in-oil emulsions of sodium polyacrylate
US4211642A (en) * 1979-01-05 1980-07-08 Vojislav Petrovich Beneficiation of coal and metallic and non-metallic ores by froth flotation process using polyhydroxy alkyl xanthate depressants
US4474619A (en) * 1979-01-25 1984-10-02 The Dow Chemical Company Conditioner for flotation of coal
EP0020275A1 (en) * 1979-06-01 1980-12-10 Calgon Corporation Process for improving the recovery of clean coal from flotation circuits
US4253944A (en) * 1979-12-28 1981-03-03 The Dow Chemical Company Conditioner for flotation of oxidized coal
US4305815A (en) * 1979-12-28 1981-12-15 The Dow Chemical Company Conditioner for flotation of oxidized coal
US4278533A (en) * 1980-02-07 1981-07-14 The Dow Chemical Company Conditioner for flotation of oxidized coal
US4537599A (en) * 1983-04-28 1985-08-27 Greenwald Sr Edward H Process for removing sulfur and ash from coal
US4604099A (en) * 1984-01-30 1986-08-05 Ciba-Geigy Corporation Process for printing cellulose-containing textile material with foam-containing reactive dyes and addition of (meth) acrylamide polymers
GB2163975A (en) * 1984-09-06 1986-03-12 American Cyanamid Co Froth flotation of coal
US4732669A (en) * 1986-07-21 1988-03-22 The Dow Chemical Company Conditioner for flotation of coal

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Brookstein et al "Foam Assisted Dewatering" Albany Int'nl Research Co. Dedham, Mass.
Brookstein et al Foam Assisted Dewatering Albany Int nl Research Co. Dedham, Mass. *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5799882A (en) * 1996-02-21 1998-09-01 Klimpel; Richard R. Hydroxy-carboxylic acid grinding aids
US6135372A (en) * 1996-02-21 2000-10-24 Klimpel; Richard R. Hydroxy-carboxylic acid grinding aids
WO2007021213A1 (en) * 2005-08-15 2007-02-22 Obschestvo S Ogranichennoy Otvetstvennostyu 'mezdunarodny Nauchny Tsentr Po Teplophizike I Energetike' Coal dressing method and device for carrying out said method
RU2500480C2 (en) * 2012-02-20 2013-12-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Иркутский государственный технический университет" (ФГБОУ ВПО "ИрГТУ") Method for extraction of nano-sized particles from man-made wastes by flotation
WO2015103316A1 (en) * 2013-12-31 2015-07-09 Omnis Mineral Technologies, Llc Vibration assisted vacuum dewatering of fine coal particles
US9587192B2 (en) 2013-12-31 2017-03-07 Earth Technologies Usa Limited Vibration assisted vacuum dewatering of fine coal particles
CN112147299A (en) * 2020-09-22 2020-12-29 中国矿业大学(北京) Method and device for detecting content of clay minerals

Similar Documents

Publication Publication Date Title
Tang et al. Removal of heavy metals with sequential sludge washing techniques using saponin: optimization conditions, kinetics, removal effectiveness, binding intensity, mobility and mechanism
US5346630A (en) Coal dewatering
US5402894A (en) Coal conditioning process
US20020108903A1 (en) Keratin protein adsorption of heavy metals
Kandah et al. The aqueous adsorption of copper and cadmium ions onto sheep manure
US6290066B1 (en) Method for removal of ammonia from fly ash
US5907037A (en) Cellulosic ion-exchange medium, and method of making and using the same
JPH06189778A (en) Biomass reaction product
CN109759024A (en) A kind of preparation method of the light sorbent based on plant cellulose
Hooper et al. Improving GAC performance by optimized coagulation
US7101524B2 (en) Process for purifying sand
JP3426234B2 (en) Method for treating combustion residues and purifying combustion fumes
RU2025148C1 (en) Method for floatation of materials containing alkali-earth metal
EP1328357B1 (en) Process for the treatment of bottom ash from waste incineration plants
AU689843B2 (en) Dewatering of alumina trihydrate
CS199718B2 (en) Process for the neutralization of rinsing water and mordants from pickling shops
JP2002355552A (en) Material and method for treating nitrogen oxide, and method of treating flue gas
CN111408479A (en) Low-rank coal flotation separation method with surface active agent adsorbed first and then desorbed under calcium ion condition
JPH05220387A (en) Deodorization and decoloration of waste water utilizing coal ash and high-grade processing agent
Matis et al. Adsorption of fatty acids on fine mineral particles as a purification method of industrial wastewaters
RU2164824C2 (en) Apatite or flotation process
JPS5817677B2 (en) Method for removing arsenic in aqueous solution
EP0069148A1 (en) Removing sulfur and beneficiating coal
Steinhilber et al. Fractionation and characterization of two aerobic sewage sludges
SU1544498A1 (en) Method of removing harmful admixtures from mineral resources

Legal Events

Date Code Title Description
AS Assignment

Owner name: CHEMICAL DEWATERING TECHNOLOGY, INC., ILLINOIS

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WINTERHOFF, MARY ANNE;REEL/FRAME:006742/0362

Effective date: 19931012

CC Certificate of correction
REMI Maintenance fee reminder mailed
FPAY Fee payment

Year of fee payment: 4

SULP Surcharge for late payment
LAPS Lapse for failure to pay maintenance fees
LAPS Lapse for failure to pay maintenance fees

Free format text: PATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20030404